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N-butane activation over ruthenium and iron promoted VPO catalysts.

The Fe- and Ru-promoted vanadium phosphorus oxide (VPO) catalysts were synthesized via the organic route in iso-butanol to form the VPO precursor, VOHPO4·0.5H2O. The resulting precursor was then activated in a stream of nitrogen to form an amorphous (VO)2P2O7, which crystallized after conditioning in the reactor in the presence of n-butane. The promoted catalysts were synthesized at 0.1%, 0.3% and 1% loading, pelletized and sieved to give a 300-600 μm pellet size. The catalysts were tested in a fixed-bed continuous flow micro-reactor and the products were analyzed by GC’s equipped with a flame ionization detector (FID) to monitor maleic anhydride and n-butane and a thermal conductivity detector (TCD) to monitor the carbon oxides. A range of characterization techniques were employed to determine the influence of the promoting elements on a VPO catalyst and to associate the composition of the catalysts obtained from such techniques with their performance. The characterization techniques used include X-ray diffraction (XRD), BET-surface area, ICP-OES, EDS, 31PNMR, TPR, redox titrations, ATR and SEM to determine the phase composition of the catalysts, the surface area of the promoted catalysts relative to the un-promoted VPO, elemental mole ratios, the reducibility of the catalysts, average vanadium oxidation state, determination of the anions present in the surface of the catalysts and the variations in the morphology of the catalysts,
respectively. Optimization of the system involved variation of the GHSV, the reactor temperature and the promoter loading. (Activation of a 0.75% n-butane in air mixture was performed at an optimum
temperature of 400oC while varying the gas hourly space velocity to establish a range of feed conversions and subsequently determine the activity of each catalyst with respect to n-butane conversion). The promoted catalysts modified the morphology of the catalysts as evidenced by the scanning electron microscopy and the X-ray diffraction patterns. Furthermore an improved conversion was obtained with these catalysts. However, only the 0.1% iron-promoted catalyst improved maleic anhydride yield leading to ca. 10% maleic anhydride yield increment. Yields of 46% and 55% were obtained at GHSVs of 2573 and 1450 per hour respectively and a temperature of 400oC. Electronic and structural modifications were encountered leading to an improved catalytic performance. The performance of this catalyst is associated with a vanadyl pyrophosphate phase (XRD), and a limited and controlled amount of V5+ species as
illustrated in the TPR, and solid state 31P NMR data. Moreover, this modification can be considered both structural and electronic in nature as observed in the SEM images and FTIR spectra of this catalyst. Furthermore, this improved performance is possible at higher conversions 80 to 90% conversion. / Thesis (M.Sc.)-University of KwaZulu-Natal, Westville, 2009.
Date January 2009
ContributorsFriedrich, Holger Bernhard.
Source SetsSouth African National ETD Portal
Detected LanguageEnglish

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